Guar gum containing compounds

ABSTRACT

Disclosed is a compound having the following structure: 
     
       
         
         
             
             
         
       
     
     where X 1  though X 10  are each independently —H, —OH, or an alkyl group and n is an integer from 2 to 100.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.13/449,239, filed Apr. 17, 2012, which is a continuation of U.S.application Ser. No. 13/219,324, filed Aug. 26, 2011 (now issued as U.S.Pat. No. 8,158,113), which is a continuation application of U.S.application Ser. No. 12/144,342 (now issued as U.S. Pat. No. 8,029,771),filed Jun. 23, 2008, which claims the benefit of U.S. ProvisionalApplication No. 60/947,199, filed Jun. 29, 2007. The contents of thereferenced applications are incorporated by reference.

BACKGROUND OF THE INVENTION

A. Field of the Invention

The present invention relates generally to a compound that can be usedas a dispersing agent or suspending agent in compositions. The compoundcan include a guar gum backbone that has selected groups attached to thebackbone.

B. Description of Related Art

Cosmetic compositions come in a wide variety of colors or shades. Thisvariety is often exhibited in products such as lipsticks, eyeliners,mascara, and blushes. Colorants such as pigments can be used to createthese different colors or shades.

A problem associated with the use of colorants is that they tend toagglomerate together in a composition. This agglomeration can cause thecolor of the composition to appear blotchy. One attempt to solve thisagglomeration problem is to either treat the surface of the colorants oradd a compound to the composition that interacts with the colorant tomore efficiently disperse the colorant throughout the composition.Although these type of treatments and compounds have been shown todecrease agglomeration, such treatments and compounds oftentimesinefficiently disperse such colorants. This can cause the composition tohave a streaky or non-homogenous color appearance.

SUMMARY OF THE INVENTION

The present invention overcomes deficiencies in the art. In anon-limiting aspect, the invention relates generally to compounds thatcan be used as dispersing and/or suspending agents. In certainembodiments, the compounds can include a guar gum backbone that includesat least one —H, —OH, an alkoxy group, an acyloxy group, an amino group,an amido group, a sulfate group, a sulfonate group, a phosphate group, aphosphonate group, or a silicone group attached to the backbone. In onenon-limiting aspect, the groups attached to the guar gum backbone can bealkyl benzoate groups, urethane groups, surfactants, silicone groups,ester groups, or combinations thereof. The ratio of the guar gumbackbone to a particular group or a combination of groups attached tothe backbone can vary to obtain a desired characteristic of thecompound. By way of example, the ratio of the guar gum backbone to aparticular group or combination of groups attached to the backbone canbe about 1:1, 2:1, 3:1, 4:1, 5:1, 6:1, 7:1, 8:1, 9:1, 10:1, 11:1, 12:1,13:1, 14:1, 15:1, 16:1, 17:1, 18:1, 19:1, 20:1, 21:1, 22:1, 23:1, 24:1,25:1, 26:1, 27:1, 28:1, 29:1, 30:1, 31:1, 32:1, 33:1, 34:1, 35:1, 36:1,37:1, 38:1, 39:1, 40:1, 50:1, 60:1, 70:1, 80:1, 90:1, 100:1, 1:2, 1:3,1:4, 1:5, 1:6, 1:7, 1:8, 1:9, 1:10, 1:11, 1:12, 1:13, 1:14, 1:15, 1:16,1:17, 1:18, 1:19, 1:20, 1:21, 1:22, 1:23, 1:24, 1:25, 1:26, 1:27, 1:28,1:29, 1:30, 1:31, 1:32, 1:33, 1:34, 1:35, 1:36, 1:37, 1:38, 1:39, 1:40,1:50, 1:60, 1:70, 1:80, 1:90, 1:100, or more or any number derivabletherein, by weight (e.g., molecular weight) of the total compound.Generic and specific structures of these compounds are disclosedthroughout this specification and incorporated into this section byreference.

In certain aspects, the compounds can have any desired molecule weight.For instance, certain compounds of the present invention can have anaverage molecular weight between 5 kilodaltons and 8,000 kilodaltons(e.g., 5, 10, 15, 20, 230, 40, 50, 60, 70, 80, 90, 100, 500, 1000, 1500,2000, 2500, 3000, 3500, 4000, 4500, 5000, 5500, 6000, 6500, 7000, 7500,8000, or more or any range or integer derivable therein). In oneembodiment, at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60,70, 80, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99% or more of the molecularweight of the compound can be attributed to the guar gum backbone, agroup attached to the backbone, or a combination of groups to thebackbone.

The compounds can be used as dispersing agents, wetting agents, orsuspending agents in compositions. In certain aspects, the compounds arecapable of decrease an amount of a colorant in a cosmetic composition byat least 1, 5, 10, 15, 20, 30, 40, 50, 60, 70, 80, 90 percent, whilemaintaining the cosmetic characteristics of the composition.

In other aspects, the compounds can be applied to the surface of acolorant, solid, particle, powder, etc. Non-limiting examples includeiron oxides, micas, and pearlescent pigments. The compounds can beattached to such surfaces by known methods (e.g., spray techniques,immersion techniques. In certain aspects, the compounds are chemicallybonded to the surface (e.g., covalent bonds, ionic bonds, etc.). Inother aspects, the compounds can be attached to the surface by the wayof an adhesive.

Another aspect of the present invention includes a composition thatincludes the guar gum containing compounds disclosed throughout thisspecification. The compositions can include a colorant, a particle, asolid, a powder etc. The composition can be cosmetic compositions,pharmaceutical compositions, ink compositions, paint compositions, etc.The composition can be topically applied to skin. The compositions canbe included in a vehicle. Non-limiting examples of cosmetic vehicles aredisclosed in other sections of this specification and are known to thoseof skill in the art. Examples of cosmetic vehicles include emulsions(e.g., oil-in-water and water-in-oil emulsions), creams, lotions,solutions (e.g., aqueous or hydro-alcoholic solutions), anhydrous bases(e.g., lipstick or a powder), gels, and ointments. In other non-limitingembodiments, the compositions of the present invention can be includedin anti-aging, cleansing, or moisturizing products. The compositions canbe anhydrous. In other aspects of the present invention, compositionscan be storage stable or color stable, or both.

In certain embodiments, the compositions of the present invention caninclude from about 1% to about 99%, by weight or volume, of the guar gumcontaining compounds. It should be recognized, however, that the amountof the compounds in a composition can be modified below, within, orabove this range based on the desired results (e.g., 1, 2, 3, 4, 5, 6,7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25,26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43,44, 45, 46, 47, 48, 49, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96, 97,98, 99%, or more, by weight or volume of the composition). In certainembodiments, the compositions of the present invention can furtherinclude a colorant, a particle, a solid, a powder etc. In certainaspects, the ratio of any ingredient within the composition whencompared to another ingredient can be from about 1:1, 2:1, 3:1, 4:1,5:1, 6:1, 7:1, 8:1, 9:1, 10:1, 11:1, 12:1, 13:1, 14:1, 15:1, 16:1, 17:1,18:1, 19:1, 20:1, 21:1, 22:1, 23:1, 24:1, 25:1, 26:1, 27:1, 28:1, 29:1,30:1, 31:1, 32:1, 33:1, 34:1, 35:1, 36:1, 37:1, 38:1, 39:1, 40:1, 50:1,60:1, 70:1, 80:1, 90:1, 100:1, or more or any number derivable therein,by weight or volume of the total composition. In other aspects, theratio of any ingredient within the composition when compared to anotheringredient can be from about 1:2, 1:3, 1:4, 1:5, 1:6, 1:7, 1:8, 1:9,1:10, 1:11, 1:12, 1:13, 1:14, 1:15, 1:16, 1:17, 1:18, 1:19, 1:20, 1:21,1:22, 1:23, 1:24, 1:25, 1:26, 1:27, 1:28, 1:29, 1:30, 1:31, 1:32, 1:33,1:34, 1:35, 1:36, 1:37, 1:38, 1:39, 1:40, 1:50, 1:60, 1:70, 1:80, 1:90,1:100, or more or any number derivable therein, by weight or volume ofthe total composition. The compositions in non-limiting aspects can havea pH of about 6 to about 9. In other aspects, the pH can be 1, 2, 3, 4,5, 6, 7, 8, 9, 10, 11, 12, 13, or 14. The compounds can be included in ahydrophobic phase e.g., oil phase, silicone phase, etc.) of acomposition. The compositions can include an effective amount of acompound to permit a high content (e.g., up to at least 30%) of acolorant in the composition or to obtain a transparent composition. Itis also contemplated that the viscosity of the composition can beselected to achieve a desired result (e.g., depending on the type ofcomposition desired, the viscosity of such composition can be from about1 cps to well over 1 million cps or any range or integer derivabletherein (e.g., 2 cps, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70,80, 90, 100, 200, 300, 400, 500, 600, 700, 800, 900, 1000, 2000, 3000,4000, 5000, 6000, 7000, 8000, 9000, 10000, 20000, 30000, 40000, 50000,60000, 70000, 80000, 90000, 100000, 200000, 300000, 400000, 500000,600000, 700000, 800000, 900000, 1000000 cps, etc.).

Various methods for using the compounds are also disclosed. By way ofexample, a method of dispersing a colorant in a composition comprisingadding a compound of the present invention to the composition, whereinthe colorant is dispersed throughout the composition is disclosed. Othermethods include a method of reducing the appearance of coloring streaksor undispersed colorants in a composition comprising adding a compoundof the present invention to the composition, wherein the appearance ofcoloring streaks or undispersed colorants in the composition is reducedwhen compared to a composition that does not include such a compound.Also disclosed is a method of increasing the viscosity of a compositioncomprising adding a compound of the present invention to thecomposition, wherein the viscosity of the composition is increased whencompared to a composition that does not include such a compound. Amethod of suspending an agent in a composition comprising adding acompound of the present invention to the composition is also disclosed.Also contemplated is a method of decreasing the amount of a colorant ina composition while maintaining the color of the composition comprisingadding the compound of claim 1 to the composition, wherein the compoundallows for the removal of at least 10% of the colorant from thecomposition while maintaining the color of the composition when comparedto the same composition that does not include such a compound. A methodof providing a homogenous color to a composition comprising adding acompound of the present invention to the composition is disclosed. Amethod of increasing the intensity of the color of a compositioncomprising adding a compound of the present invention to thecomposition, where the color intensity of the composition is increasedwhen compared to a composition that does not include such a compound isalso disclosed. There is also disclosed a method of obtaining atransparent composition comprising adding a compound of the presentinvention to the composition. In another aspect, there is disclosed amethod of increasing the dispersibility or decreasing the agglomerationof a colorant, a particle, a solid, a powder, etc. in a compositioncomprising applying a compound of the present invention to the surfaceof the colorant, particle, solid, powder, etc., wherein thedispersibility of the colorant, particle, solid, powder, etc. in thecomposition is increased or the agglomeration of the same is decreasedwhen compared with the dispersibility or agglomeration of such acolorant, particle, solid, powder, etc., in a composition that does nothave the compound attached to its surface.

Also contemplated are methods of treating or preventing a skin conditioncomprising topical application of a composition of the present inventionto skin, wherein the topical application of the composition treats theskin condition. Non-limiting examples of skin conditions includepruritus, spider veins, lentigo, age spots, senile purpura, keratosis,melasma, blotches, fine lines or wrinkles, nodules, sun damaged skin,dermatitis (including, but not limited to seborrheic dermatitis,nummular dermatitis, contact dermatitis, atopic dermatitis, exfoliativedermatitis, perioral dermatitis, and stasis dermatitis), psoriasis,folliculitis, rosacea, acne, impetigo, erysipelas, erythrasma, eczema,and other inflammatory skin conditions. In certain non-limiting aspects,the skin condition can be caused by exposure to UV light, age,irradiation, chronic sun exposure, environmental pollutants, airpollution, wind, cold, heat, chemicals, disease pathologies, smoking, orlack of nutrition. The skin can be facial skin or non-facial skin (e.g.,arms, legs, hands, chest, back, feet, etc.). The method can furthercomprise identify a person in need of skin treatment. The person can bea male or female.

Also contemplated are kits that include the compositions of the presentinvention. In certain embodiments, the composition is comprised in acontainer. The container can be a bottle, dispenser, or package. Thecontainer can dispense a pre-determined amount of the composition. Incertain aspects, the compositions is dispensed in a spray or mist,dollop, or liquid. The container can include indicia on its surface. Theindicia can be a word, an abbreviation, a picture, or a symbol.

Also contemplated is a product comprising a composition of the presentinvention. In non-limiting aspects, the product can be a cosmeticproduct. The cosmetic product can be those described in other sectionsof this specification or those known to a person of skill in the art.Non-limiting examples of products include a moisturizer, a cream, alotion, a skin softener, a foundation, a night cream, a lipstick, acleanser, a toner, a sunscreen, a mask, or an anti-aging product.

It is contemplated that any embodiment discussed in this specificationcan be implemented with respect to any method or composition of theinvention, and vice versa. Furthermore, compositions of the inventioncan be used to achieve methods of the invention.

“Alkyl” includes straight-chain alkyl groups, branched-chain alkylgroups, cycloalkyl (alicyclic) groups, alkyl heteroatom-substitutedcycloalkyl groups, cycloalkyl heteroatom-substituted alkyl groups,heteroatom-unsubstituted C_(n)-alkyl, and heteroatom-substitutedC_(n)-alkyl groups.

“Heteroatom-unsubstituted C_(n)-alkyl” includes a radical, having alinear or branched, cyclic or acyclic structure, further having nocarbon-carbon double or triple bonds, further having a total of n carbonatoms, all of which are nonaromatic, 3 or more hydrogen atoms, and noheteroatoms. For example, a heteroatom-unsubstituted C₁-C₁₀-alkyl has 1to 10 carbon atoms. The groups, —CH₃, —CH₂CH₃, —CH₂CH₂CH₃, —CH(CH₃)₂,—CH(CH₂)₂ (cyclopropyl), —CH₂CH₂CH₂CH₃, —CH(CH₃)CH₂CH₃, —CH₂CH(CH₃)₂,—C(CH₃)₃, —CH₂C(CH₃)₃, cyclobutyl, cyclopentyl, and cyclohexyl, are allnon-limiting examples of heteroatom-unsubstituted alkyl groups.

“Heteroatom-substituted C_(n)-alkyl” includes a radical, having a singlesaturated carbon atom as the point of attachment, no carbon-carbondouble or triple bonds, further having a linear or branched, cyclic oracyclic structure, further having a total of n carbon atoms, all ofwhich are nonaromatic, 0, 1, or more than one hydrogen atom, at leastone heteroatom, wherein each heteroatom is independently selected fromthe group consisting of N, O, F, Cl, Br, I, Si, P, and S. For example, aheteroatom-substituted C₁-C₁₀-alkyl has 1 to 10 carbon atoms. Thefollowing groups are all non-limiting examples of heteroatom-substitutedalkyl groups: trifluoromethyl, —CH₂F, —CH₂Cl, —CH₂Br, —CH₂OH, —CH₂OCH₃,—CH₂OCH₂CH₃, —CH₂OCH₂CH₂CH₃, —CH₂OCH(CH₃)₂, —CH₂OCH(CH₂)₂, —CH₂OCH₂CF₃,—CH₂OCOCH₃, —CH₂NH₂, —CH₂NHCH₃, —CH₂N(CH₃)₂, —CH₂NHCH₂CH₃,—CH₂N(CH₃)CH₂CH₃, —CH₂NHCH₂CH₂CH₃, —CH₂NHCH(CH₃)₂, —CH₂NHCH(CH₂)₂,—CH₂N(CH₂CH₃)₂, —CH₂CH₂F, —CH₂CH₂Cl, —CH₂CH₂Br, —CH₂CH₂I, —CH₂CH₂OH,CH₂CH₂OCOCH₃, —CH₂CH₂NH₂, —CH₂CH₂N(CH₃)₂, —CH₂CH₂NHCH₂CH₃,—CH₂CH₂N(CH₃)CH₂CH₃, —CH₂CH₂NHCH₂CH₂CH₃, —CH₂CH₂NHCH(CH₃)₂,—CH₂CH₂NHCH(CH₂)₂, —CH₂CH₂N(CH₂CH₃)₂, —CH₂CH₂NHCO₂C(CH₃)₃, and—CH₂Si(CH₃)₃.

“Alkoxy” includes a group having the structure —OR, where R is an alkylgroup.

“Acyl” includes straight-chain acyl groups, branched-chain acyl groups,cycloacyl (alicyclic) groups, acyl heteroatom-substituted cycloacylgroups, cycloacyl heteroatom-substituted acyl groups,heteroatom-unsubstituted C_(n)-acyl, and heteroatom-substitutedC_(n)-acyl groups.

“Heteroatom-unsubstituted C_(n)-acyl” refers to a radical, having asingle carbon atom of a carbonyl group as the point of attachment,further having a linear or branched, cyclic or acyclic structure,further having a total of n carbon atoms, 1 or more hydrogen atoms, atotal of one oxygen atom, and no additional heteroatoms. For example, aheteroatom-unsubstituted C₁-C₁₀-acyl has 1 to 10 carbon atoms. Thegroups, —CHO, —COCH₃, —COCH₂CH₃, COCH₂CH₂CH₃, —COCH(CH₃)₂, —COCH(CH₂)₂,—COC₆H₅, —COC₆H₄CH₃, —COC₆H₄CH₂CH₃, —COC₆H₄CH₂CH₂CH₃, —COC₆H₄CH(CH₃)₂,—COC₆H₄CH(CH₂)₂, and —COC₆H₃(CH₃)₂, are non-limiting examples ofheteroatom-unsubstituted acyl groups.

“Heteroatom-substituted C_(n)-acyl” refers to a radical, having a singlecarbon atom as the point of attachment, the carbon atom being part of acarbonyl group, further having a linear or branched, cyclic or acyclicstructure, further having a total of n carbon atoms, 0, 1, or more thanone hydrogen atom, at least one additional heteroatom in addition to theoxygen of the carbonyl group, wherein each additional heteroatom isindependently selected from the group consisting of N, O, F, Cl, Br, I,Si, P, and S. For example, a heteroatom-substituted C₁-C₁₀-acyl has 1 to10 carbon atoms. The term heteroatom-substituted acyl includescarbamoyl, thiocarboxylate, and thiocarboxylic acid groups. The groups,—COCH₂CF₃, —CO₂H, —CO₂CH₃, —CO₂CH₂CH₃, —CO₂CH₂CH₂CH₃, CO₂CH(CH₃)₂,—CO₂CH(CH₂)₂, —CONH₂, —CONHCH₃, —CONHCH₂CH₃, —CONHCH₂CH₂CH₃,—CONHCH(CH₃)₂, —CONHCH(CH₂)₂, —CON(CH₃)₂, —CON(CH₂CH₃)CH₃, —CON(CH₂CH₃)₂and —CONHCH₂CF₃, are examples heteroatom-substituted acyl groups.

“Acyloxy” includes a group having the structure —OR, where R is an acylgroup.

“Amido” includes N-alkyl-amido, N-aryl-amido, N-aralkyl-amido,acylamino, alkylcarbonylamino, arylcarbonylamino, ureido groups,heteroatom-unsubstituted C_(n)-amido, or heteroatom-substitutedC_(n)-amido.

“Heteroatom-unsubstituted C_(n)-amido” includes a radical, having asingle nitrogen atom as the point of attachment, further having acarbonyl group attached via its carbon atom to the nitrogen atom,further having a linear or branched, cyclic or acyclic structure,further having a total of n carbon atoms, 1 or more hydrogen atoms, atotal of one oxygen atom, a total of one nitrogen atom, and noadditional heteroatoms. For example, a heteroatom-unsubstitutedC₁-C₁₀-amido has 1 to 10 carbon atoms.

“Heteroatom-substituted C_(n)-amido” includes a radical, having a singlenitrogen atom as the point of attachment, further having a carbonylgroup attached via its carbon atom to the nitrogen atom, further havinga linear or branched, cyclic or acyclic structure, further having atotal of n aromatic or nonaromatic carbon atoms, 0, 1, or more than onehydrogen atom, at least one additional heteroatom in addition to theoxygen of the carbonyl group, wherein each additional heteroatom isindependently selected from the group consisting of N, O, F, Cl, Br, I,Si, P, and S. For example, a heteroatom-substituted C₁-C₁₀-amido has 1to 10 carbon atoms.

“Sulfonate” groups includes the general formula RSO₂O⁻, where R is anorganic group, including any of those identified throughout thespecification.

“Sulfate” groups includes the general formula ROSO₂O⁻ where R isindependently —H or an organic group, including any of those identifiedthroughout the specification.

“Phosphonate” groups includes the general formula OP(OR)₂R where R isindependently —H or an organic group, including any of those identifiedthroughout the specification.

“Phosphate” groups includes the general formula OP(OR₃) where R isindependently —H or an organic group, including any of those identifiedthroughout the specification.

The term “about” or “approximately” are defined as being close to asunderstood by one of ordinary skill in the art, and in one non-limitingembodiment the terms are defined to be within 10%, within 5%, within 1%,and/or within 0.5%.

The terms “inhibiting,” “preventing,” or “reducing,” or any variation ofthese terms, when used in the claims and/or the specification includesany measurable decrease or complete inhibition to achieve a desiredresult.

The term “effective,” as that term is used in the specification and/orclaims, means adequate to accomplish a desired, expected, or intendedresult.

The use of the word “a” or “an” when used in conjunction with the term“comprising” in the claims and/or the specification may mean “one,” butit is also consistent with the meaning of “one or more,” “at least one,”and “one or more than one.”

The use of the term “or” in the claims is used to mean “and/or” unlessexplicitly indicated to refer to alternatives only or the alternativesare mutually exclusive, although the disclosure supports a definitionthat refers to only alternatives and “and/or.”

As used in this specification and claim(s), the words “comprising” (andany form of comprising, such as “comprise” and “comprises”), “having”(and any form of having, such as “have” and “has”), “including” (and anyform of including, such as “includes” and “include”) or “containing”(and any form of containing, such as “contains” and “contain”) areinclusive or open-ended and do not exclude additional, unrecitedelements or method steps.

Other objects, features and advantages of the present invention willbecome apparent from the following detailed description. It should beunderstood, however, that the detailed description and the examples,while indicating specific embodiments of the invention, are given by wayof illustration only. Additionally, it is contemplated that changes andmodifications within the spirit and scope of the invention will becomeapparent to those skilled in the art from this detailed description.

DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS

The guar gum containing compounds of the present invention have a guargum backbone with selected R groups attached to the backbone. Guar Gumis a glactomannan polymer that can be extracted from the seed of thelguminous shrub Cyamopsis tetragonoloba. This plant is typicallycultivated in India, Pakistan, and southwestern U.S. The CAS registrynumber for guar gum is 9000-30-0. Guar gum is commercially availablefrom a variety of sources (e.g., Tic Gums—Belcamp Md., and RhodiaInc—Cranbury N.J.). Non-limiting examples of R groups include —H, —OH,an alkoxy group, an acyloxy group, an amino group, an amido group, asulfate group, a sulfonate group, a phosphate group, a phosphonategroup, or a silicone group. The selected R groups can modify or providedesired characteristics to the guar gum compound. By way of exampleonly, some desired characteristics include dispersion and/or suspensioncapabilities when the modified compound is used in a given compositionor a phase of a composition.

When the compounds of the present invention are used as a dispersionagent, they can be used to disperse colorants or other solid ingredientsefficiently throughout the composition or a phase of the composition(e.g., a hydrophobic phase of a water-in-oil or oil-in-water emulsion).An advantage of having efficient dispersion of a colorant is that it canreduce the appearance of undeveloped colors in the composition. Thecomposition can have a homogenous color appearance. Because of theefficient dispersion, more colorant can be added to the compositionwithout affecting the stability of the composition which can be usefulin obtaining a true or more intense, vivid, or vibrant color. When usedas a suspending agent, the compounds can effectively modify theviscosity of the composition. For instance, the compounds can be used toincrease the viscosity of a composition to achieve a desired rheologicalcharacteristic.

These and other aspect of the invention are described in furthernon-limiting detail below.

A. Guar Gum Containing Compounds

The guar gum containing compounds of the present invention can include aguar gum backbone that includes at least one —H, —OH, an alkoxy group,an acyloxy group, an amino group, an amido group, an ester group, asulfate group, a sulfonate group, a phosphate group, a phosphonategroup, a silicone group, a surfactant, a urethane group (includingpolyurethanes) attached to the backbone. A non-limiting genericstructure of such a compound is illustrated below:

where: R₁ through R₉ are each independently —H, —OH, an alkoxy group, anacyloxy group, an amino group, an amido group, an ester group, a sulfategroup, a sulfonate group, a phosphate group, a phosphonate group, asurfactant, a urethane group (including polyurethanes), or a siliconegroup having the following structure:

where R₁₀ though R₁₁ are each independently —H or an alkyl group; and nand o are independently integers from 2 to 10,000, where at least one ofR₁ through R₉ is an alkoxy group, an acyloxy group, an amino group, anamido group, an ester group, a sulfate group, a sulfonate group, aphosphate group, a phosphonate group, a surfactant, a urethane group(including polyurethanes), or a silicone group.

Non-limiting examples of particular compounds of the present inventionare illustrated below. These compounds have alkyl benzoate groups and/orsilicone groups attached the guar gum backbone:

where X₁ though X₁₀ are each independently —H, —OH, or an alkyl group;and n is an integer from 2 to 100.

where Y₁ though Y₄ are each independently —H or an alkyl group; and n,o, and p are independently integers from 2 to 100.

where X₁ though X₅ are each independently —H, —OH, or an alkyl group; Y₃though Y₄ are each independently —H or an alkyl group; and n and p areindependently integers from 2 to 100.

where Y₁ though Y₂ are each independently —H or an alkyl group; X₆though X₁₀ are each independently —H, —OH, or an alkyl group; and n ando are independently integers from 2 to 100.

B. Modifications and Derivatives of the Guar Gum Compounds

Modifications or derivatives of the guar gum containing compoundsdisclosed throughout this specification are contemplated as being usefulwith the methods and compositions of the present invention. Derivativesand modifications may be prepared and the properties of such derivativesand modified compounds may be assayed for their desired properties byany method known to those of skill in the art. The modifications orderivatives can be made by using convention chemical synthesistechniques (see, e.g., Organic Chemistry, 5^(th) Ed.).

In certain aspects, “derivative” refers to a chemically modified guargum containing compound that still retains the desired effects of thecompound prior to the chemical modification. Such derivatives may havethe addition, removal, or substitution of one or more chemical moietieson the guar gum backbone and/or the R groups that are attached to thebackbone. Non-limiting examples of the modifications that can be made tothese portions of the compounds include the addition or removal of alkylgroups, carboxyl groups, carbonyl groups, hydroxyl groups, nitro groups,amino groups, amide groups, azo groups, sulfate groups, sulfonategroups, sulfono groups, sulfhydryl groups, sulfonyl groups, sulfoxidogroups, phosphate groups, phosphono groups, phosphoryl groups, and/orhalide groups. Additional modifications can include an addition or adeletion of one or more atoms of the atomic framework, for example,substitution of an ethyl by a propyl or substitution of a phenyl by alarger or smaller aromatic group. In a cyclic or bicyclic structure,hetero atoms such as N, S, or O can be substituted into the structureinstead of a carbon atom.

C Compositions

The compounds of the present invention can be incorporated into alltypes of compositions (e.g., cosmetic and pharmaceutical compositions).A person of ordinary skill would recognize that the compositions caninclude any number of combinations of the guar gum containing compoundsand/or additional ingredients, or derivatives thereof. Theconcentrations of the guar gum containing compounds and/or additionalingredients, or derivatives thereof, can vary for a given composition.This variation can oftentimes depend on the desired characteristics ofthe final composition. In non-limiting embodiments, for example, thecompositions may include in their final form, for example, at leastabout 0.0001%, 0.0002%, 0.0003%, 0.0004%, 0.0005%, 0.0006%, 0.0007%,0.0008%, 0.0009%, 0.0010%, 0.0011%, 0.0012%, 0.0013%, 0.0014%, 0.0015%,0.0016%, 0.0017%, 0.0018%, 0.0019%, 0.0020%, 0.0021%, 0.0022%, 0.0023%,0.0024%, 0.0025%, 0.0026%, 0.0027%, 0.0028%, 0.0029%, 0.0030%, 0.0031%,0.0032%, 0.0033%, 0.0034%, 0.0035%, 0.0036%, 0.0037%, 0.0038%, 0.0039%,0.0040%, 0.0041%, 0.0042%, 0.0043%, 0.0044%, 0.0045%, 0.0046%, 0.0047%,0.0048%, 0.0049%, 0.0050%, 0.0051%, 0.0052%, 0.0053%, 0.0054%, 0.0055%,0.0056%, 0.0057%, 0.0058%, 0.0059%, 0.0060%, 0.0061%, 0.0062%, 0.0063%,0.0064%, 0.0065%, 0.0066%, 0.0067%, 0.0068%, 0.0069%, 0.0070%, 0.0071%,0.0072%, 0.0073%, 0.0074%, 0.0075%, 0.0076%, 0.0077%, 0.0078%, 0.0079%,0.0080%, 0.0081%, 0.0082%, 0.0083%, 0.0084%, 0.0085%, 0.0086%, 0.0087%,0.0088%, 0.0089%, 0.0090%, 0.0091%, 0.0092%, 0.0093%, 0.0094%, 0.0095%,0.0096%, 0.0097%, 0.0098%, 0.0099%, 0.0100%, 0.0200%, 0.0250%, 0.0275%,0.0300%, 0.0325%, 0.0350%, 0.0375%, 0.0400%, 0.0425%, 0.0450%, 0.0475%,0.0500%, 0.0525%, 0.0550%, 0.0575%, 0.0600%, 0.0625%, 0.0650%, 0.0675%,0.0700%, 0.0725%, 0.0750%, 0.0775%, 0.0800%, 0.0825%, 0.0850%, 0.0875%,0.0900%, 0.0925%, 0.0950%, 0.0975%, 0.1000%, 0.1250%, 0.1500%, 0.1750%,0.2000%, 0.2250%, 0.2500%, 0.2750%, 0.3000%, 0.3250%, 0.3500%, 0.3750%,0.4000%, 0.4250%, 0.4500%, 0.4750%, 0.5000%, 0.5250%, 0.0550%, 0.5750%,0.6000%, 0.6250%, 0.6500%, 0.6750%, 0.7000%, 0.7250%, 0.7500%, 0.7750%,0.8000%, 0.8250%, 0.8500%, 0.8750%, 0.9000%, 0.9250%, 0.9500%, 0.9750%,1.0%, 1.1%, 1.2%, 1.3%, 1.4%, 1.5%, 1.6%, 1.7%, 1.8%, 1.9%, 2.0%, 2.1%,2.2%, 2.3%, 2.4%, 2.5%, 2.6%, 2.7%, 2.8%, 2.9%, 3.0%, 3.1%, 3.2%, 3.3%,3.4%, 3.5%, 3.6%, 3.7%, 3.8%, 3.9%, 4.0%, 4.1%, 4.2%, 4.3%, 4.4%, 4.5%,4.6%, 4.7%, 4.8%, 4.9%, 5.0%, 5.1%, 5.2%, 5.3%, 5.4%, 5.5%, 5.6%, 5.7%,5.8%, 5.9%, 6.0%, 6.1%, 6.2%, 6.3%, 6.4%, 6.5%, 6.6%, 6.7%, 6.8%, 6.9%,7.0%, 7.1%, 7.2%, 7.3%, 7.4%, 7.5%, 7.6%, 7.7%, 7.8%, 7.9%, 8.0%, 8.1%,8.2%, 8.3%, 8.4%, 8.5%, 8.6%, 8.7%, 8.8%, 8.9%, 9.0%, 9.1%, 9.2%, 9.3%,9.4%, 9.5%, 9.6%, 9.7%, 9.8%, 9.9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%,17%, 18%, 19%, 20%, 21%, 22%, 23%, 24%, 25%, 26%, 27%, 28%, 29%, 30%,35%, 40%, 45%, 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, or 99% orany range derivable therein, of at least one of the guar gum containingcompound and/or additional ingredients, or derivatives thereof. Incertain non-limiting aspects, the percentages can be calculated byweight or volume of the total composition. A person of ordinary skill inthe art would understand that the concentrations can vary depending onthe addition, substitution, and/or subtraction of the guar gumcontaining compound and additional ingredients, or derivatives thereof.

D Additional Ingredients

In addition to the guar gum containing compounds disclosed throughoutthis specification, compositions of the present invention can includeadditional ingredients such as cosmetic ingredients and pharmaceuticalactive ingredients. Non-limiting examples of these additionalingredients are described in the following subsections.

1. Cosmetic Ingredients

The CTFA International Cosmetic Ingredient Dictionary and Handbook(2004) describes a wide variety of non-limiting cosmetic ingredientsthat can be used in the context of the present invention. Examples ofthese ingredient classes include: fragrances (artificial and natural),dyes and color ingredients (e.g., Blue 1, Blue 1 Lake, Red 40, titaniumdioxide, D&C blue no. 4, D&C green no. 5, D&C orange no. 4, D&C red no.17, D&C red no. 33, D&C violet no. 2, D&C yellow no. 10, and D&C yellowno. 11), adsorbents, lubricants, solvents, moisturizers (including,e.g., emollients, humectants, film formers, occlusive agents, and agentsthat affect the natural moisturization mechanisms of the skin),water-repellants, UV absorbers (physical and chemical absorbers such asparaminobenzoic acid (“PABA”) and corresponding PABA derivatives,titanium dioxide, zinc oxide, etc.), essential oils, vitamins (e.g. A,B, C, D, E, and K), trace metals (e.g. zinc, calcium and selenium),anti-irritants (e.g. steroids and non-steroidal anti-inflammatories),botanical extracts (e.g. aloe vera, chamomile, cucumber extract, ginkgobiloba, ginseng, and rosemary), anti-microbial agents, antioxidants(e.g., BHT and tocopherol), chelating agents (e.g., disodium EDTA andtetrasodium EDTA), preservatives (e.g., methylparaben andpropylparaben), pH adjusters (e.g., sodium hydroxide and citric acid),absorbents (e.g., aluminum starch octenylsuccinate, kaolin, corn starch,oat starch, cyclodextrin, talc, and zeolite), skin bleaching andlightening agents (e.g., hydroquinone and niacinamide lactate),humectants (e.g., sorbitol, urea, and manitol), exfoliants,waterproofing agents (e.g., magnesium/aluminum hydroxide stearate), skinconditioning agents (e.g., aloe extracts, allantoin, bisabolol,ceramides, dimethicone, hyaluronic acid, and dipotassium glycyrrhizate).Non-limiting examples of some of these ingredients are provided in thefollowing subsections.

a. Colorants

In certain non-limiting aspects, the guar gum containing compounds canbe used to efficiently disperse colorants throughout a compositionand/or a phase (e.g., water, oil, silicone phase) of the composition.Non-limiting examples of colorants that can be used in the context ofthe present invention include those known to a person of ordinary skillin the art (see, e.g., CTFA International Cosmetic Ingredient Dictionaryand Handbook (2004)). For instance natural and synthetic pigments andlakes can be used. Examples of groups of pigments include carbon,cadmium, iron oxide, Prussian blue, chromium, cobalt, copper, titanium,ultramarine, zinc, clay earth, and organic pigments. Specificnon-limiting examples of colorants include Aluminum Powder, Blue 1 Lake,Bronze Powder, Chromium Oxide Greens, Copper Powder, Ext. Yellow 7 Lake,Green 3 Lake, Orange 4 Lake, Orange 5 Lake, Orange 10 Lake, Pigment Blue15, Pigment Blue 15:2, Pigment green 7, Pigment Orange 5, Pigment Red 4,Pigment Red 5, Pigment Red 48, Pigment Red 53, Pigment Red 53:1, PigmentRed 57, Pigment Red 57:1, Pigment Red 63:1, Pigment Red 64:1, PigmentRed 68, Pigment Red 83, Pigment Red 88, Pigment Red 90:1 Aluminum Lake,Pigment Red 112, Pigment Red 172 Aluminum Lake, Pigment Red 173 AluminumLake, Pigment Red 190, Pigment Violet 19, Pigment Yellow 1, PigmentYellow 3, Pigment Yellow 12, Pigment Yellow 13, Pigment Yellow 73, Red 4Lake, Red 6 Lake, Red 7 Lake, Red 21 Lake, Red 22 Lake, Red 27 Lake, Red28 Lake, Red 30 Lake, Red 31 Lake, Red 33 Lake, Red 34 Lake, Red 36Lake, Red 40 Lake, Sunset Yellow Aluminum Lake, Yellow 5 Lake, Yellow 6Lake, Yellow 7 Lake, Yellow 10 Lake, and Zinc Oxide.

b. Preservatives

Non-limiting examples of preservatives that can be used in the contextof the present invention include quaternary ammonium preservatives(e.g., polyquaternium-1), parabens (e.g., methylparabens andpropylparabens), phenoxyethanol, benzyl alcohol, chlorobutanol, phenol,sorbic acid, thimerosal or combinations thereof.

c. Moisturizers

Non-limiting examples of moisturizing agents that can be used with thecompositions of the present invention can be found in the InternationalCosmetic Ingredient Dictionary, 10^(th) Ed., 2004. Examples includeamino acids, chondroitin sulfate, diglycerin, erythritol, fructose,glucose, 1,2,6-hexanetriol, honey, hyaluronic acid, hydrogenated honey,hydrogenated starch hydrolysate, inositol, lactitol, maltitol, maltose,mannitol, natural moisturizing factor, salts of pyrollidone carboxylicacid, potassium PCA, sodium glucuronate, sodium PCA, sorbitol, sucrose,trehalose, urea, xylitol, glycerin, and petrolatum.

d. Emollients

Non-limiting examples of emollients include, but are not limited to,vegetable oils, mineral oils, silicone oils, synthetic and naturalwaxes, petrolatum, lanolin, aluminum magnesium hydroxide stearate (whichcan also function as a water repellent), and fatty acid esters.Non-limiting examples of vegetable oils include safflower oil, corn oil,sunflower seed oil, olive oil, or joboba esters.

e. Antioxidants

Non-limiting examples of antioxidants include, but are not limited to,acetyl cysteine, ascorbic acid, ascorbic acid polypeptide, ascorbyldipalmitate, ascorbyl methylsilanol pectinate, ascorbyl palmitate,ascorbyl stearate, BHA, BHT, t-butyl hydroquinone, cysteine, cysteineHCl, diamylhydroquinone, di-t-butylhydroquinone, dicetylthiodipropionate, dioleyl tocopheryl methylsilanol, disodium ascorbylsulfate, distearyl thiodipropionate, ditridecyl thiodipropionate,dodecyl gallate, erythorbic acid, esters of ascorbic acid, ethylferulate, ferulic acid, gallic acid esters, hydroquinone, isooctylthioglycolate, magnesium ascorbate, magnesium ascorbyl phosphate,methylsilanol ascorbate, natural botanical anti-oxidants such as greentea or grape seed extracts, nordihydroguaiaretic acid, octyl gallate,phenylthioglycolic acid, potassium ascorbyl tocopheryl phosphate,potassium sulfite, propyl gallate, quinones, rosmarinic acid, sodiumascorbate, sodium bisulfate, sodium erythorbate, sodium metabisulfite,sodium sulfite, superoxide dismutase, sodium thioglycolate, sorbitylfurfural, thiodiglycol, thiodiglycolamide, thiodiglycolic acid,thioglycolic acid, thiolactic acid, thiosalicylic acid, tocophereth-5,tocophereth-10, tocophereth-12, tocophereth-18, tocophereth-50,tocopherol, tocophersolan, tocopheryl acetate, tocopheryl linoleate,tocopheryl nicotinate, tocopheryl succinate, andtris(nonylphenyl)phosphite.

f. Thickening Agents

Thickening agents, including thickener or gelling agents, includesubstances which that can increase the viscosity of a composition.Thickeners include those that can increase the viscosity of acomposition without substantially modifying the efficacy of theingredients within the composition. Thickeners can also increase thestability of the compositions of the present invention. Non-limitingexamples of additional thickeners that are known to those of ordinaryskill in the art can be used in the context of the present invention(e.g., U.S. Pat. Nos. 5,087,445; 4,509,949; 2,798,053; InternationalCosmetic Ingredient Dictionary and Handbook, 10^(th) Ed., 2004).Examples include carboxylic acid polymers, crosslinked polyacrylatepolymers, polyacrylamide polymers, polysaccharides, and gums. Examplesof carboxylic acid polymers include crosslinked compounds containing oneor more monomers derived from acrylic acid, substituted acrylic acids,and salts and esters of these acrylic acids and the substituted acrylicacids, wherein the crosslinking agent contains two or more carbon-carbondouble bonds and is derived from a polyhydric alcohol. Examples ofcommercially available carboxylic acid polymers include carbomers, whichare homopolymers of acrylic acid crosslinked with allyl ethers ofsucrose or pentaerytritol (e.g., Carbopol™ 900 series from B. F.Goodrich).

g. Silicone Containing Compounds

In non-limiting aspects, silicone containing compounds include anymember of a family of polymeric products whose molecular backbone ismade up of alternating silicon and oxygen atoms with side groupsattached to the silicon atoms. By varying the —Si—O— chain lengths, sidegroups, and crosslinking, silicones can be synthesized into a widevariety of materials. They can vary in consistency from liquid to gel tosolids.

The silicone containing compounds that can be used in the context of thepresent invention include those described in this specification or thoseknown to a person of ordinary skill in the art. Non-limiting examplesinclude silicone oils (e.g., volatile and non-volatile oils), gels, andsolids. The silicon containing compound can be a silicone oil such as apolyorganosiloxane. Non-limiting examples of polyorganosiloxanes includedimethicone, cyclomethicone, polysilicone-11, phenyl trimethicone,trimethylsilylamodimethicone, stearoxytrimethylsilane, or mixtures ofthese and other organosiloxane materials in any given ratio in order toachieve the desired consistency and application characteristicsdepending upon the intended application (e.g., to a particular area suchas the skin, hair, or eyes). A “volatile silicone oil” includes asilicone oil have a low heat of vaporization, i.e. normally less thanabout 50 cal per gram of silicone oil. Non-limiting examples of volatilesilicone oils include: cyclomethicones such as Dow Corning 344 Fluid,Dow Corning 345 Fluid, Dow Corning 244 Fluid, and Dow Corning 245 Fluid,Volatile Silicon 7207 (Union Carbide Corp., Danbury, Conn.); lowviscosity dimethicones, i.e. dimethicones having a viscosity of about 50cst or less (e.g., dimethicones such as Dow Corning 200-0.5 cst Fluid).The Dow Corning Fluids are available from Dow Corning Corporation,Midland, Mich. Cyclomethicone and dimethicone are described inInternational Cosmetic Ingredient Dictionary, 10^(th) Ed., 2004 ascyclic dimethyl polysiloxane compounds and a mixture of fully methylatedlinear siloxane polymers end-blocked with trimethylsiloxy units,respectively. Other non-limiting volatile silicone oils that can be usedin the context of the present invention include those available fromGeneral Electric Co., Silicone Products Div., Waterford, N.Y. and SWSSilicones Div. of Stauffer Chemical Co., Adrian, Mich.

2. Pharmaceutical Actives

Pharmaceutical active agents are also contemplated as being useful withthe compositions of the present invention. Non-limiting examples ofpharmaceutical active agents include anti-acne agents, agents used totreat rosacea, analgesics, anesthetics, anorectals, antihistamines,anti-inflammatory agents including non-steroidal anti-inflammatorydrugs, antibiotics, antifungals, antivirals, antimicrobials, anti-canceractives, scabicides, pediculicides, antineoplastics, antiperspirants,antipruritics, antipsoriatic agents, antiseborrheic agents, biologicallyactive proteins and peptides, burn treatment agents, cauterizing agents,depigmenting agents, depilatories, diaper rash treatment agents,enzymes, hair growth stimulants, hair growth retardants including DFMOand its salts and analogs, hemostatics, kerotolytics, canker soretreatment agents, cold sore treatment agents, dental and periodontaltreatment agents, photosensitizing actives, skin protectant/barrieragents, steroids including hormones and corticosteroids, sunburntreatment agents, sunscreens, transdermal actives, nasal actives,vaginal actives, wart treatment agents, wound treatment agents, woundhealing agents, etc.

E Vehicles

Compositions of the present invention can be incorporated into all typesof vehicles. Non-limiting examples of suitable vehicles includeemulsions (e.g., water-in-oil, water-in-oil-in-water, oil-in-water,oil-in-water-in-oil, oil-in-water-in-silicone, water-in-silicone,silicone-in-water emulsions), creams, lotions, solutions (both aqueousand hydro-alcoholic), anhydrous bases (such as lipsticks and powders),gels, and ointments or by other method or any combination of theforgoing as would be known to one of ordinary skill in the art (see,e.g., Remington's, 1990 and International Cosmetic Ingredient Dictionaryand Handbook, 10^(th) Ed., 2004)). Variations and other appropriatevehicles will be apparent to the skilled artisan and are appropriate foruse in the present invention. In certain aspects, it is important thatthe concentrations and combinations of the compounds, ingredients, andagents be selected in such a way that the combinations are chemicallycompatible and do not form complexes which precipitate from the finishedproduct.

F Cosmetic Products and Articles of Manufacture

The composition of the present invention can also be used in manycosmetic products including, but not limited to, sunscreen products,sunless skin tanning products, hair products, finger nail products,moisturizing creams, skin benefit creams and lotions, softeners, daylotions, gels, ointments, foundations, night creams, lipsticks,cleansers, toners, masks, or other known cosmetic products orapplications. Additionally, the cosmetic products can be formulated asleave-on or rinse-off products. In certain aspects, the compositions ofthe present invention are stand-alone products.

G Kits

Kits are also contemplated as being used in certain aspects of thepresent invention. For instance, emulsion compositions of the presentinvention can be included in a kit. A kit can include a container.Containers can include a bottle, a metal tube, a laminate tube, aplastic tube, a dispenser, a pressurized container, a barrier container,a package, a compartment, a lipstick container, a compact container,cosmetic pans that can hold cosmetic compositions, or other types ofcontainers such as injection or blow-molded plastic containers intowhich the dispersions or compositions or desired bottles, dispensers, orpackages are retained. The kit and/or container can include indicia onits surface. The indicia, for example, can be a word, a phrase, anabbreviation, a picture, or a symbol.

The containers can dispense a pre-determined amount of the emulsioncomposition. In other embodiments, the container can be squeezed (e.g.,metal, laminate, or plastic tube) to dispense a desired amount of theemulsion composition. The emulsion composition can be dispensed as aspray, an aerosol, a liquid, a fluid, or a semi-solid. The containerscan have spray, pump, or squeeze mechanisms. A kit can also includeinstructions for employing the kit components as well the use of anyother emulsion compositions included in the container. Instructions caninclude an explanation of how to apply, use, and maintain the emulsioncompositions.

EXAMPLES

The following examples are included to demonstrate certain non-limitingaspects of the invention. It should be appreciated by those of skill inthe art that the techniques disclosed in the examples which followrepresentative techniques discovered by the inventor to function well inthe practice of the invention. However, those of skill in the art shouldappreciate that changes can be made in the specific embodiments whichare disclosed and still obtain a like or similar result withoutdeparting from the spirit and scope of the invention.

Example 1 Determining Efficacy of the Guar Gum Containing Compounds asDispersing Agents

The efficacy of the guar gum containing compounds disclosed throughoutthis specification as dispersing agents can be determined by methodsknown to those of ordinary skill in the art. For instance a Hegamandraw-down gauge or a Colorimetric/spectroscopic evaluation (%reflectance vs. wavelength) can be used to measure the dispersion of acolorant in a composition or a phase of a composition. The agglomerationof a colorant can also be analyzed by reviewing the distribution curveof such a colorant in a composition or a phase of a composition.

All of the compounds, compositions, and/or methods disclosed and claimedcan be made and executed without undue experimentation in light of thepresent disclosure. While the compounds, compositions, and methods ofthis invention have been described in terms of certain embodiments, itwill be apparent to those of skill in the art that variations may beapplied to the compounds, compositions, and/or methods and in the stepsor in the sequence of steps of the method without departing from theconcept, spirit and scope of the invention. More specifically, it willbe apparent that certain agents which are both chemically andphysiologically related may be substituted for the agents describedherein while the same or similar results would be achieved. All suchsimilar substitutes and modifications apparent to those skilled in theart are deemed to be within the spirit, scope and concept of theinvention.

REFERENCES

The following references, to the extent that they provide exemplaryprocedural or other details supplementary to those set forth herein, arespecifically incorporated herein by reference.

-   U.S. Pat. No. 2,798,053-   U.S. Pat. No. 4,509,949-   U.S. Pat. No. 5,087,445-   CTFA International Cosmetic Ingredient Dictionary and Handbook,    10^(th) Ed., (2004). Organic Chemistry, 5^(th) Ed.-   Remington's Pharmaceutical Sciences, 18th Ed. Mack Printing Company,    1289-1329, 1990.

1. A compound having the following structure:

where X₁ though X₁₀ are each independently —H, —OH, or an alkyl group;and n is an integer from 2 to
 100. 2. The compound of claim 1, whereinX₁ though X₁₀ are each —H.
 3. The compound of claim 1, further comprisedin a cosmetic composition.
 4. The compound of claim 3, wherein thecosmetic composition is a mascara, an eyeliner, or a lipstick.